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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951496Generated: October 26, 2026

2-Fluoroaniline → N-(2-fluorophenyl)-3-[(8aS)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamide

https://huagongshe.com/reaction/1951496

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoroanilineHCID 9584—
ReactantBenzoyl chloride, 3-(chlorosulfonyl)-HCID 77671—
Reactant(6S)-1,4-Diazabicyclo(4.3.0)nonaneHCID 781249—
SolventDichloromethaneHCID 6344—
ProductN-(2-fluorophenyl)-3-[(8aS)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamideHCID 46851310—

Reaction Steps

To 3-(chlorosulfonyl)benzoyl chloride (0.521 g, 2.18 mmol) in anhydrous dichloromethane (10 mL) was added (S)-octahydropyrrolo[1,2-α]pyrazine (0.250 g, 1.98 mmol) in dichloromethane (4 mL) slowly over 10 minutes at room temperature. The mixture was stirred at room temperature for 5 hours. Then 2-fluoroaniline (1.54 g, 13.87 mmol) was added. The mixture was stirred at room temperature overnight and then concentrated. The residue was purified by chromatography on silica gel (dichloromethane, then methanol/dichloromethane=1:10) to give the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404719B2
Source datasetuspto-grants-2013_03
ORD IDord-f9268048856541ff90bf2e35d795b084
Source noteuspto-grants-2013_03